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144446-23-1

β-aflatrem is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 144446-23-1 Structure

  • Basic information

    1. Product Name: β-aflatrem
    2. Synonyms:
    3. CAS NO:144446-23-1
    4. Molecular Formula:
    5. Molecular Weight: 501.666
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 144446-23-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: β-aflatrem(CAS DataBase Reference)
    10. NIST Chemistry Reference: β-aflatrem(144446-23-1)
    11. EPA Substance Registry System: β-aflatrem(144446-23-1)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 144446-23-1(Hazardous Substances Data)

144446-23-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 144446-23-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,4,4 and 6 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 144446-23:
(8*1)+(7*4)+(6*4)+(5*4)+(4*4)+(3*6)+(2*2)+(1*3)=121
121 % 10 = 1
So 144446-23-1 is a valid CAS Registry Number.

144446-23-1Downstream Products

144446-23-1Relevant articles and documents

Nodulisporic acid e biosynthesis:: In vivo characterisation of NodD1, an indole-diterpene prenyltransferase that acts on an emindole SB derived indole-diterpene scaffold

Van De Bittner, Kyle C.,Cameron, Rosannah C.,Bustamante, Leyla Y.,Bundela, Rudranuj,Kessans, Sarah A.,Vorster, Jan,Nicholson, Matthew J.,Parker, Emily J.

, p. 1160 - 1164 (2019/07/25)

Prenylation of aromatic compounds is a key tailoring reaction in biosynthesis of bioactive indole-diterpenes. Here, we identify NodD1 as the enzyme responsible for the bisprenylation of nodulisporic acid F. This prenyltransferase showed a preference for its natural indole-diterpene substrate whereas other related enzymes were not able to catalyse this conversion.

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